F5 gene HR2 haplotype [Genotype] in Blood by Molecular genetics method Nominal 93788-8
LOINC Code
| LOINC code | 93788-8 | ||
|---|---|---|---|
| name | F5 gene HR2 haplotype [Genotype] in Blood by Molecular genetics method Nominal | ||
| description | Factor V HR2 Allele, DNA Mutation Analysis is useful in patients who are carriers of Factor V Mutation (Leiden)as coinheritance of Factor V Mutation (Leiden) is associated with a 3-4-fold increased risk of venous thrombosis compared to inheritance of Factor V Mutation (Leiden) alone. As a result the result of the HR2 haplotype analysis is interpreted in the context of knowledge of the Leiden mutation. | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | F5 gene HR2 haplotype | ||
| property | Geno = Genotype | ||
| time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||
| system | Bld = Whole blood | ||
| scale | Nom = Nominal: Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody. | ||
| method | Molgen = Molecular Genetics: General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods. | ||
Additional Names | |||
| short name | F5 HR2 Geno Bld | ||
Basic Attributes | |||
| class | MOLPATH | ||
| type | 1 Laboratory | ||
| order vs. observation | Both | ||
Associated Observations | |||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||
History/Usage | |||
| first released | |||
| last updated | 2.68 | ||
| last change type | MIN - change to field other than name | ||
Related Names | |||
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